Increased expression of native cytosolic Cu/Zn superoxide dismutase and ascorbate peroxidase improves tolerance to oxidative and chilling stresses in cassava (Manihot esculenta Crantz)
© Xu et al. 2014
Received: 30 May 2014
Accepted: 22 July 2014
Published: 5 August 2014
Cassava (Manihot esculenta Crantz) is a tropical root crop, and is therefore, extremely sensitive to low temperature; its antioxidative response is pivotal for its survival under stress. Timely turnover of reactive oxygen species (ROS) in plant cells generated by chilling-induced oxidative damages, and scavenging can be achieved by non-enzymatic and enzymatic reactions in order to maintain ROS homeostasis.
Transgenic cassava plants that co-express cytosolic superoxide dismutase (SOD), MeCu/ZnSOD, and ascorbate peroxidase (APX), MeAPX2, were produced and tested for tolerance against oxidative and chilling stresses. The up-regulation of MeCu/ZnSOD and MeAPX2 expression was confirmed by the quantitative reverse transcriptase-polymerase chain reaction, and enzymatic activity analyses in the leaves of transgenic cassava plant lines with a single-transgene integration site. Upon exposure to ROS-generating agents, 100 μM ROS-generating reagent methyl viologen and 0.5 M H2O2, higher levels of enzymatic activities of SOD and APX were detected in transgenic plants than the wild type. Consequently, the oxidative stress parameters, such as lipid peroxidation, chlorophyll degradation and H2O2 synthesis, were lower in the transgenic lines than the wild type. Tolerance to chilling stress at 4°C for 2 d was greater in transgenic cassava, as observed by the higher levels of SOD, catalase, and ascorbate-glutathione cycle enzymes (e.g., APX, monodehydroascorbate reductase, dehydroascorbate reducatase and glutathione reductase) and lower levels of malondialdehyde content.
These results suggest that the expression of native cytosolic SOD and APX simultaneously activated the antioxidative defense mechanisms via cyclic ROS scavenging, thereby improving its tolerance to cold stress.
Cassava (Manihot esculenta Crantz) is an important tropical root crop that plays an important role not only in ensuring food security, but also in various bioindustrial applications such as animal feed, modified starch and biofuels ,. Because cassava is native to tropical regions, it is extremely cold-sensitive; its growth is drastically affected at temperatures lower than 18°C, and the plant cannot survive for long after exposure to freezing conditions –. Therefore, low temperatures and freezing conditions are the most important limiting factors for the cultivating location, as well as productivity. The damage of apical shoot seems be to more critical than other parts of the cassava plant . Improving the tolerability of the cassava plant to multiple stresses has therefore, become a major objective of cassava breeders, especially in subtropical regions ,. Under cold conditions, up-regulation of reactive oxygen species (ROS) turnover and scavenging in cassava has been reported, and therefore, genetic manipulation of intracellular ROS level might be an effective approach in improving tolerance to abiotic stresses in this tropical crop –.
In the ROS scavenging system that is responsible for homeostasis in plant cells, superoxide dismutases (SODs, EC 184.108.40.206), enzymes that catalyze the dismutation of superoxide into oxygen and hydrogen peroxide, provide the first line of defense against ROS in various subcellular compartments, i.e. chloroplast, mitochondria and cytosol . Essentially, there are three types of SODs, each containing either manganese, iron, or copper plus zinc as a prosthetic group . Along with other ROS scavenging mechanisms like catalase (CAT; EC 220.127.116.11), glutathione peroxidases (GPXs) and peroxiredoxin reductases (PrxRs), and the ascorbate–glutathione (ASC-GSH) cycle, the ROS levels are maintained in a homeostatic state. In the ASC-GSH cycle, using ascorbate as an electron donor, ascorbate peroxidase (APX, EC 18.104.22.168) scavenges potentially harmful hydrogen peroxide to water from the chloroplasts and mitochondria, as well as other organelles ,. Therefore, the formation of toxic hydroxyl radicals by superoxide and hydrogen peroxide can be controlled by the combined enzymatic actions of SOD and APX .
Transgenic plants that express SOD or APX have shown enhanced tolerance to multiple stresses . For example, over-expression of different SODs (FeSOD, MnSOD or Cu/ZnSOD) in transgenic plants of tomato, rice, poplar, alfalfa, etc., showed increased tolerance to methyl viologen (MV), ozone, high salinity, chilling or other stresses –. Transgenic plants have also demonstrated an increased tolerance against various abiotic stresses by the expression of either cytosolic- or organelle-targeted cytosolic APX –. However, some reports suggest no change in response to oxidative or environmental stress with the expression of a single antioxidant enzyme ,. These contradictory findings may be due to the complex network of plant antioxidant defenses, which possibly confer a higher tolerance to oxidative stress by pyramiding or stacking of multiple genes in a single genotype . The gene-stacking approach entails manipulation of two or more desirable enzymes mediating the ROS turnover and scavenging pathways, in improving the abiotic stress tolerance in plants.
Indeed, co-expression of two distinct ROS-scavenging enzymes, such as SOD and other ROS-scavenging enzymes, in the chloroplasts or cytosol in transgenic plants has a synergistic effect in increasing the levels of abiotic stress resistance. For example, coupled expression of Cu/ZnSOD and APX in transgenic plants of Festuca arundinacea, potato, tobacco, sweet potato and plum led to increased tolerance to multiple abiotic stresses, e.g., the herbicide methyl viologen (MV), chilling, high temperature and drought ,–. Payton et al.  showed that co-expression of glutathione reductase (GR, EC 22.214.171.124) and APX in cotton improved antioxidant enzyme activity during moderate chilling at high light intensity, in chloroplasts . Co-expression of the Suaeda salsa glutathione S-transferase (GST) and CAT1 in rice also caused tolerance to stresses caused by salt and paraquat . Taken together, these data indicated that the combination of transgenes encoding different ROS-scavenging enzymes in various subcellular compartments might have a synergistic effect in improving stress tolerance.
Lately, plant breeders and biotechnologists have appreciated the molecular insights and advances in cassava abiotic stress resistance, on a global scale. Apart from the various approaches from traditional breeding to field evaluation , studies of cassava response to drought or cold stress at the molecular level have reportedly used the “omics” technology, e.g., expressed sequence tags, cDNAs and oligonucleotide microarray ,–. However, few studies on improved tolerance to environmental stresses using genetic engineering have been reported ,. Senescence-induced expression of the isopentenyl transferase gene in cassava showed increased drought resistance, as observed by the elevated content of cytokinin in mature leaves, and prolonged leaf life . Enhanced ROS scavenging by simultaneous expression of cytosolic MeCu/ZnSOD and peroxisomal MeCAT1 in transgenic cassava also confirmed the improved tolerance towards drought and cold temperatures .
In the present study, transgenic cassava plants co-expressing both cytosolic MeCu/ZnSOD (Genbank accession No. AY642137) and cytosolic MeAPX2 (GenBank accession No. AY973622) showed enhanced ROS scavenging capacity, thereby leading to enhanced tolerance to oxidative stresses that was induced by MV, H2O2 as well as chilling. Our results suggest that manipulation of ROS-scavenging enzyme systems by the overexpression of both cytosolic SOD and APX is a worthwhile approach to produce transgenic plants with enhanced tolerance to a wide range of abiotic stresses.
Subcellular localization of MeCu/ZnSOD and MeAPX2
Green fluorescent protein (GFP) was the fusion protein used for subcellular localization of MeCu/ZnSOD and MeAPX2. The control, CaMV 35S-eGFP construct, exhibited GFP fluorescence in the cytoplasm and nucleus of agroinfiltrated cells of N. benthamiana leaves. The MeCu/ZnSOD has been reported as a cytosolic SOD isoform in our previous report . The MeAPX2 was located in the cytosol of the leaf cells, as indicated by the fused GFP fluorescence (Additional file 1) that was consistent with the signal peptide sequences predicted by Reilly et al. . Therefore, both enzymes used in the study were cytosolic proteins.
Molecular characterization of the transgenic plants
Higher protoplast viability and mitochondrial integrity of mesophyll cells under H2O2stress
Enhanced tolerance to H2O2-mediated oxidative stress in transgenic leaves
The activities of SOD and APX in cassava leaves were assessed under normal and stressful conditions (Figure 4c, d). Enzyme activities were not significantly different between WT and transgenic plants under normal conditions. However, after stress induction, the SOD activity of WT plants decreased to 20% of the baseline value in 24 hours (1.7 U mg−1 protein, Figure 4c). In contrast, the SOD activity of all transgenic plant lines increased in 12 hours; for example, the activity level in SA4 showed a 2-fold increase as compared to 0 hours with 23.4 U mg−1 protein. However, their activities decreased at 24 hours; the lowest value was observed in SA1 plants with 6.6 U mg−1 protein, which was about 4-times higher than that of WT plants (Figure 4c). A consistent increase in APX activity was detected in all leaves, especially in SA1, with the activity level showing a 3-fold increased at 24 h as compared to 0 h; protein levels increased from 0.06 μmol · min−1 · mg−1 protein to 0.33 μmol · min−1 · mg−1 protein. The WT only showed an increase from 0.05 μmol · min−1 · mg−1 protein to 0.17 μmol · min−1 · mg−1 protein. At 24 hours, all transgenic plant leaves showed a significant increase in activity compared to the WT plant leaves (Figure 4d).
Enhanced tolerance to methyl viologen (MV)-mediated oxidative stress in transgenic leaves
Improved cold tolerance of transgenic plants
The cassava plant is generally considered to be cold-sensitive, and abiotic stresses, such as low temperature and salinity, dramatically affect their growth, thereby, leading to reduced productivity ,. Excessive ROS generation, which might result in hypersensitive response and cell death in cassava, has been identified as an important indicator of such conditions ,. Therefore, maintaining ROS homeostasis via ROS production and scavenging mechanisms is critical ,. Optimum regulation of ROS generation and scavenging by the mobilization of various pathways has been proposed as a vital mechanism for managing stress in cassava ,, and our previous study had confirmed that increased resistance to abiotic stress could be achieved in transgenic cassava by over-expression of cytosolic Cu/ZnSOD and peroxisomal CAT1 ,. In this study, we showed that transgenic cassava with coupled expression of cytosolic MeCu/ZnSOD and cytosolic MeAPX2 leads to improved oxidative and chilling stress resistance through elevated ROS scavenging. Our studies confirmed that the response to abiotic stress can be improved in cassava by genetic engineering techniques that combine two different ROS-scavenging pathways, i.e., SOD/CAT and SOD/ASC-GSH cycle.
Most of ROS scavenging enzymes co-expressed targeted the chloroplast –. Recently, Faize et al.  and Diaz-Vivancos et al.  reported that over-expression of cytosolic SOD and APX in tobacco and plums improved drought and salt tolerance. An interesting question raised is the effectiveness of the stacked ROS-scavenging enzymes with various subcellular targeting strategies in plants, undoubtedly their individual important function in stress defense ,. Since the substrate for APX activity is H2O2 that is a by-product of SOD action, their individual functions should be combined to achieve a synergistic effect on stress tolerance. Indeed, upon chilling, the enzymatic activity of MDHAR, DHAR and GR in the ASC-GSH cycle in the transgenic cassava was significantly increased (Figure 7). We noticed that, comparing to the transgenic cassava overexpressed cytosolic SOD and peroxisomal CAT , the SA transgenic cassava showed less tolerance to post-harvest physiological deterioration of their storage roots (data not shown). We suppose that the PPD occurrence in cassava storage root is directly linked to the oxidization process in the subcellular organelles of parenchyma cells; the action of in the peroxisome enables the timely scavenging of excess ROS generated in situ.
Both H2O2 and MV treatment in the presence of light lead to the generation of superoxide radicals and H2O2 in chloroplasts and mitochondria of plants. In vivo imaging of ROS using the fluorescent probe rhodamine-123, a stain readily sequestered by active mitochondria and mesophyll protoplasts, or DAB staining of cassava leaves showed improved tolerance of transgenic cassava cells to oxidative stress caused by H2O2 and MV (Figures 3, 4). At the cellular level, the viability of the mesophyll protoplast and integrity of the mitochondrial were clearly indicated by their tolerance to H2O2 in transgenic cassava cells (Figure 3). These results indicate that transgenic plants expressing both cytosolic SOD and cytosolic APX are able to rapidly scavenge superoxide and hydrogen peroxide at the site of generation, as well as prevent the formation of hydroxyl radicals, the most toxic ROS, prior to their interaction with target molecules, as noted in our previous report . The changes were observed not only in cytosolic antioxidant system but also in the chloroplasts and mitochondria, which implied that changes in the cytosolic antioxidant defense impacts the subcellular compartments, consistent with previous reports ,,,. Therefore, ROS scavenging system in plant cells is an integrative network for developing an antioxidant machinery through cytosol and subcellular organelle interactions.
Under cold conditions, non-transformed cassava plants showed signs of oxidative stress-induced cellular damage such as wilting, and increased lipid peroxidation of leaves (Figure 6). Cassava is very sensitive to low temperature; cold temperatures disrupt the metabolic balance of plant cells, resulting in enhanced production of ROS, e.g. H2O2. The timely detoxification of ROS is necessary for the maintenance of the Calvin cycle and transpiration . Transcriptome profiling of low temperature-exposed cassava showed an increase in transcripts and enzyme activities of ROS scavenging genes and the accumulation of total soluble sugars . In the SA transgenic lines, we confirmed that the enzyme activity of SOD and APX were significantly higher than that of WT during cold treatment (Figure 7). Increased catalytic activity of APX eliminated the endogenous H2O2 via the ASC-GSH cycle, which involves GR, DHAR and MDHAR, to restore the cellular redox state, thus, suggesting that the performance of ascorbate-glutathione cycle is essential for the regulation of an efficient system for scavenging the accumulated ROS in leaves during chilling stress. This response was correlated with the up-regulation of APX activity and by maintenance of ASC-GSH redox pools in cold-acclimated plants .
A higher CAT activity was also observed in the SA lines under stress conditions. This increase seemed to be involved in the removal of excess H2O2. Dong et al.  reported that peroxisomal metabolism responded to cold regulation through ROS by increasing the H2O2 production in the peroxisome . H2O2 could also diffuse through the peroxisomal membrane into the cytosol , thus increasing the risk of oxidative damage in this compartment. It suggests that ROS scavenging system in cassava is a complex network involving multiple components of ROS production, turnover and scavenging as well as their cross-interactions.
In conclusion, our results show the important role of cytosolic MeCu/ZnSOD and cytosolic MeAPX2 in cassava in improving ROS scavenging, thereby leading to reduced H2O2 accumulation and improved abiotic stress resistance. The results also confirm that the transgenic approach is effective in improving the stress resistance in cassava via proper gene stacking of ROS scavenging enzymes.
Plasmid constructions, cassava transformation and phenotype evaluation of transgenic cassava
The cDNA amplification of cassava Cu/ZnSOD (GenBank accession no. AY642137) and cassava APX2 (GenBank accession no. AY973622) was determined by PCR using primers covering the full length of transcripts. The PCR fragment was sequenced and cloned into the binary vector pCAMBIA1301 under the control of vascular-specific promoter p54/1.0 promoter (GenBank accession no. AY217353.1)  and the ubiquitous CaMV 35S promoter, respectively to generate pC-P54::MeCu/ZnSOD-35S::MeAPX2 (Figure 1a). The plasmid was mobilized into Agrobacterium tumefaciens strain LBA4404 for cassava transformation using friable embryogenic callus of cultivar TMS60444. Embryogenic callus induction of cassava TMS60444, Agrobacterium-mediated genetic transformation and plantlet regeneration were performed by the methods described by Zhang et al. .
The uniform stem cuttings of field-grown cassava plants were used for phenotype and yield evaluation. Ten stem cuttings per transgenic line and WT were planted in late spring of 2012 in Wushe Plantation for Transgenic Crops, Shanghai, China, and harvested in early November, 2012. The performance of field plants was recorded regularly till harvest.
The MeAPX2 genes tagged with green fluorescent protein (GFP) were cloned into pCAMBIA1301, and the resulting constructs were used to transform Agrobacterium tumefaciens LBA4404. To identify the subcellular localization of the gene, N. benthamiana leaves were agroinfiltrated with the Agrobacterium strains harboring pC-35::MeAPX2-eGFP binary vectors, respectively, by the protocol described previously . At 36 hours post-infiltration, the transiently transformed leaves were observed under a confocal microscope (FluoView FV1000, Olympus, Japan).
Southern blot and Real-time RT-PCR analyses of transgenic cassava plants
Southern blot analysis entailed digestion of the genomic DNA (20 μg) of cassava leaves of in vitro plants with XbaI, followed by 0.8% (w/v) agarose gel electrophoresis and subsequent transfer to a positively charged nylon membrane (Roche, Mannheim, Germany). The PCR fragment of MeAPX2 (1 Kb) was labeled with digoxigenin (DIG) using the PCR DIG Probe Synthesis Kit (Roche, Mannheim, Germany). Hybridization and detection were performed by using the DIG-High Prime DNA Labeling and Detection Starter Kit II (Roche, Mannheim, Germany), according to the manufacturer’s instructions.
Gene expression was analyzed by real-time RT-PCR (qRT-PCR) of transgenic plants. Briefly, total RNA was extracted from fresh cassava leaves of in vitro plants using the RNA Plant plus Reagent (Tiangen, Beijing, China) essentially as described previously . The RNA samples were digested with DNase I and the first strand of cDNA was synthesized from 5 μg total RNA from each sample using M-MLV reverse transcriptase (Toyobo, Osaka, Japan). qRT-PCR was carried out using the Bio-Rad CFX96 thermocycler SYBR Green I Master Mix (Toyobo, Osaka, Japan) according to the manufacturer’s protocol, under the following PCR conditions: 95°C for 1 minute, followed by 40 cycles at 95°C for 15 seconds, 60°C for 15 seconds and 72°C for 20 seconds. The qRT-PCR primers were designed using Primer 3 Plus Software (http://www.primer3plus.com). The primers were: MeCu/ZnSOD (forward 5′- ATGTTCATGCCCTTGGAGAC -3′ and reverse 5′- GATCACCAGCATGACGAATG -3′), MeAPX2 (forward 5′- CATTGATAAGGCCAGGAGGA -3′ and reverse 5′- TTGTTAGCAGCATGACCCTG - 3′), and β-actin (forward 5′- TGATGAGTCTGGTCCATCCA -3′ and reverse 5′- CCTCCTACGACCCAATCTCA -3′). Fold changes of RNA transcripts were calculated by the 2-ΔΔCt method  with β-actin as an internal control . A detailed method for qRT-PCR analysis is available in Additional file 3.
Isolation and viability assay of cassava mesophyll protoplasts
In vitro-cultured cassava seedlings were grown at 25°C with light at 200 μmol · m−2 · s−2 and a photoperiod 16 hour/8 hour (light/dark). Protoplasts were isolated from the mature leaves of 30-day-old sterile plants, as described by Anthony et al. . Leaves were sliced into 2 mm to 3 mm thin strips and incubated in digestion mixture (pH 5.8) containing 9% (w/v) mannitol, 1% Cellulose R-10 (Yakult Honsha Co., Tokyo, Japan), 1.5% macerozyme R-10 (Yakult Honsha Co., Ltd., Tokyo, Japan) and 25 mM morpholine ethanesulfonic acid (MES) in cell protoplast washing (CPW) medium (27.2 mg of KH2PO4, 101 mg of KNO3, 1480 mg of CaCl2 · 2H2O, 246 mg of MgSO4 · 7H2O, 0.16 mg of KI, 0.025 mg of CuSO4 · 5H2O per liter). After purification, the protoplasts were resuspended in CPW solution supplemented with 9% mannitol (CPW9M, pH 7.0) to a final concentration of 2 × 105 cells/mL.
Protoplast viability was determined by fluorescein diacetate (FDA) staining . The purified mesophyll protoplasts were treated for 5 minutes with CPW 9 M solution (pH 7.0) supplemented with 1 M H2O2 for 5 min, and then stained with FDA at a final concentration of 0.01%. Stained protoplasts were observed for fluorescence under a fluorescent microscope (Nikon TE2000-S, Japan). The viable percentage = (the number of protoplasts with green fluorescence)/(the number of total mesophyll protoplasts) × 100%.
Analysis of mitochondrial integrity
Mitochondrial integrity was measured by rhodamine 123 (Rh 123, Molecular Probes-Invitrogen CA, USA) fluorescence  after cassava mesophyll protoplasts were treated with 1 M H2O2 for 5 min. Fluorescence was detected using a confocal laser scanning microscope (FluoView FV1000, Olympus, Japan) with Ex/Em of 488 nm/515 nm. In each sample, 20–25 cells were scanned and viewed.
Treatment with MV, H2O2and cold
Fully expanded, healthy leaves were excised from the one-month-old plants in greenhouse and put in 10 cm-diameter petri dishes with different chemical solutions. For the MV treatment, leaves were allowed to float on 50 mL of 100 μM MV, and for the H2O2 treatment, leaves were exposed to 50 mL of 0.5 M H2O2. Leaves were incubated at 25°C under light conditions.
Four-week-old seedlings of transgenic and the control plants were transplanted into pots (30 cm in diameter, 45 cm in height) and grown in a greenhouse (16 h days, 30°C days and 22°C nights). Two-month-old plants were subjected to stress conditions. For cold treatment, plants with a uniform growth status were transferred to a chamber and incubated at 4°C for 48 hours under weak light (cool-white fluorescent light at approximately 35 μmol · m−2 · s−1).
Determination of chlorophyll content and lipid peroxidation
Chlorophyll was isolated from WT and transgenic leaf segments according to the procedure described by Arnon et al. . One-gram leaf disks from the one-month-old plants were homogenized in 10 mL of absolute ethyl alcohol and the homogenate was centrifuged at 3500 × g for 5 minutes. The supernatant was retained and the absorbance was recorded at 663 nm and 646 nm using a Nano-Drop spectrophotometer (Thermo Scientific, Scientific, Wilmington, DE, USA). Lipid peroxidation in leaf tissues was measured in terms of MDA content in the samples, according to method described by Heath and Packer . One-gram leaves were homogenized in 10 mL of 10% (w/v) trichloroacetate (TCA) and centrifuged at 10,000 × g for 10 minutes. Thereafter, 2 mL of 10% trichloroacetic acid containing 0.67% (w/v) thiobarbituric acid was added to 2 mL of the supernatant. The mixture was boiled for 15 min, quickly cooled on ice, and centrifuged at 10,000 × g for 5 minutes. The absorbance of the supernatant was recorded at 532 nm and corrected for non-specific turbidity by subtracting the absorbance at 600 nm using a Nano-Drop spectrophotometer (Thermo Scientific).
Determination of H2O2content and 3,3′-diaminobenzidine staining
After determining the lipid peroxidation as above, the quantitative measurement of H2O2 in the leaves was carried out according to the method reported by Velikova et al. . The 3,3′-diaminobenzidine (DAB) staining method was used to qualitatively detect the H2O2 generation in leaves after treatments, using the method described by Thordal-Christensen et al. .
SOD isoenzyme was analyzed by separating the protein extracts in 10% native polyacrylamide gel with a 4% stacking gel in standard tris-glycine buffer (pH 8.3). Samples were electrophoresed at 100 V through the stacking gel for 20 min and 120 V through the separating gel for 60 min. After electrophoresis, the gel was immersed in 0.1% (w/v) nitroblue tetrazolium (NBT) solution for 15 min, briefly washed in ddH2O, then immersed in 100 mM potassium phosphate buffer (pH 7.0) containing 0.028 mM riboflavin and 28 mM TEMED (N,N,N#,N#-tetramethyl-ethylenediamine) for another 15 min. Gels were briefly washed in ddH2O and illuminated on a light box, with a light intensity of 30 mE · m−2 · s−1 for 15 min to initiate the photochemical reaction .
SOD activity was detected according to the method of Beauchamp and Fridovich . A 3-mL reaction mixture contained 50 mM potassium phosphate buffer (pH 7.8), 13 mM methionine, 75 mM nitroblue tetrozulium (NBT), 2 mM riboflavin, 0.1 mM EDTA, and 100 mL enzyme extract. The reaction was initiated by placing the tubes under light intensity of 5000 lx. The absorbance was measured at 560 nm in a spectrophotometer and one unit of SOD is defined as the amount required to inhibit the photo reduction of NBT by 50%.
To analyze the APX isozymes, the protein extracts were separated in 10% native polyacrylamide gels with a 5% stacking gel in standard tris-glycine buffer with 2 mM ascorbate (pH 8.3). Samples were electrophoresed under conditions similar to the SOD isozyme electrophoresis. After electrophoresis, the gels were immersed in 50 mM potassium phosphate buffer, pH 7.0, containing 2 mM ascorbate for 10 min; then in 50 mM potassium phosphate buffer, pH 7.0, containing 4 mM ascorbate and 1 mM H2O2 for 20 min. After rinsing in water, the gels were stained in 50 mM potassium phosphate buffer, pH 7.8, containing 14 mM TEMED and 2.45 mM NBT for 10–30 min .
APX activity was determined as described by Nakano and Asada . The reaction mixture contained 50 mmol/L potassium phosphate, pH 7.0, 1 mmol/L ascorbic acid (AsA), 2.5 mmol/L H2O2 and enzyme source (ca 15 μg protein) in a final volume of 2 mL at 25°C. Ascorbate oxidation was measured spectrophotometrically by a decrease of A290, using the absorption coefficient of 2.8 mM−1 · cm−1.
The activities of monodehydroascorbate reductase (MDHAR, EC 126.96.36.199), dehydroascorbate reductase (DHAR, EC 188.8.131.52), and GR were assayed as described previously –. Protein was estimated according to Bradford .
All data were represented as mean ± SD from at least three independent experiments with three replicates. Statistical analysis was done using SPSS 15.0 for Windows (SPSS, Chicago, IL), with two-tailed Student’s t-tests for measuring significance. Double asterisks indicate significant differences between transgenic lines and WT at 1% level, one asterisk stands for at 5% level.
This work was supported by grants from the National Basic Research Program (2010CB126605), the National Natural Science Foundation of China (31271775), the National High Technology Research and Development Program of China (2012AA101204), the SIPPE-SCBG Joint Fund, the Earmarked Fund for China Agriculture Research System (CARS-12) and Shanghai Municipal Afforestation & City Appearance and Environmental Sanitation Administration (G102410, F132427).
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